Literature DB >> 18604693

A rare case of Pfeiffer's syndrome.

P Pallagatti1, S Sankaran, P Kollipara.   

Abstract

Entities:  

Mesh：

Year:  2008        PMID： 18604693     DOI： 10.1080/01443610802141134

Source DB:  PubMed          Journal:  J Obstet Gynaecol        ISSN： 0144-3615            Impact factor:   1.246


× No keyword cloud information.
  1 in total

1.  De Novo Heterozygous Mutation in FGFR2 Causing Type II Pfeiffer Syndrome.

Authors:  Rafat Mosalli; Alfia Fatma; Mohammed A Almatrafi; Mayada Mazroua; Bosco Paes
Journal:  Case Rep Genet       Date:  2022-06-28
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.